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Executive Director, Global Medical Affairs

Executive Director, Global Medical Affairs

Hydrogen GroupTrenton, NJ, US
30+ days ago
Job type
  • Full-time
Job description

Executive Director, Global Medical Affairs

Executive Director, Global Medical Affairs

3 days ago Be among the first 25 applicants

  • Lead and manage the Global Medical Affairs team, ensuring alignment with corporate goals.
  • Lead Advisory Board meetings according to the Global Medical Plan (GMP).
  • Develop and implement Global Medical Affairs strategies to support the company's product portfolio.
  • Lead the Global Medical Affairs Plan creation in collaboration with the cross-functional team.
  • Collaborate with cross-functional teams, including R&D, Regulatory Affairs, Market Access, Marketing, and Commercial teams, to ensure cohesive and effective communication strategies.
  • Oversee the development and dissemination of scientific and medical information to healthcare professionals, regulatory authorities, payors, and other stakeholders.
  • Provide medical and scientific expertise to support clinical development, regulatory submissions, and post-marketing activities.
  • Monitor and analyze industry trends, competitive landscape, and emerging scientific data to inform strategic decisions.
  • Establish and maintain relationships with key opinion leaders, healthcare professionals, and industry organizations.
  • Represent the company at scientific conferences, meetings, and other external events.
  • Ensure compliance with all relevant regulations and guidelines, including GCP, and other industry standards.
  • Manage Medical Affairs budget in alignment with forecast.

Job Description :

  • Lead and manage the Global Medical Affairs team, ensuring alignment with corporate goals.
  • Lead Advisory Board meetings according to the Global Medical Plan (GMP).
  • Develop and implement Global Medical Affairs strategies to support the company's product portfolio.
  • Lead the Global Medical Affairs Plan creation in collaboration with the cross-functional team.
  • Collaborate with cross-functional teams, including R&D, Regulatory Affairs, Market Access, Marketing, and Commercial teams, to ensure cohesive and effective communication strategies.
  • Oversee the development and dissemination of scientific and medical information to healthcare professionals, regulatory authorities, payors, and other stakeholders.
  • Provide medical and scientific expertise to support clinical development, regulatory submissions, and post-marketing activities.
  • Monitor and analyze industry trends, competitive landscape, and emerging scientific data to inform strategic decisions.
  • Establish and maintain relationships with key opinion leaders, healthcare professionals, and industry organizations.
  • Represent the company at scientific conferences, meetings, and other external events.
  • Ensure compliance with all relevant regulations and guidelines, including GCP, and other industry standards.
  • Manage Medical Affairs budget in alignment with forecast.
  • Qualifications :

  • MD, PhD, or PharmD with a strong background in Medical Affairs, and Clinical Development.
  • Over 5 years Medical Affairs experience within Oncology with at least 10 years of industry experience.
  • Developing and implementing successful Medical Affairs strategies.
  • Excellent communication, leadership, and interpersonal skills.
  • Strong knowledge of regulatory requirements.
  • Must have Oncology experience

    Seniority level

    Seniority level

    Executive

    Employment type

    Employment type

    Full-time

    Job function

    Job function

    Research and Science

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